Home / Publications / Synthesis of amidoalkyl naphthols by an iodine-catalyzed multicomponent reaction of β-naphthol

Synthesis of amidoalkyl naphthols by an iodine-catalyzed multicomponent reaction of β-naphthol

Rahul R Nagawade 1
Rahul R Nagawade
Devanand B Shinde 1
Devanand B Shinde
Published 2007-09-12
CommunicationVolume 17, Issue 5, 299-300
24
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Nagawade R. R., Shinde D. B. Synthesis of amidoalkyl naphthols by an iodine-catalyzed multicomponent reaction of β-naphthol // Mendeleev Communications. 2007. Vol. 17. No. 5. pp. 299-300.
GOST all authors (up to 50) Copy
Nagawade R. R., Shinde D. B. Synthesis of amidoalkyl naphthols by an iodine-catalyzed multicomponent reaction of β-naphthol // Mendeleev Communications. 2007. Vol. 17. No. 5. pp. 299-300.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.mencom.2007.09.018
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2007.09.018
TI - Synthesis of amidoalkyl naphthols by an iodine-catalyzed multicomponent reaction of β-naphthol
T2 - Mendeleev Communications
AU - Nagawade, Rahul R
AU - Shinde, Devanand B
PY - 2007
DA - 2007/09/12
PB - Mendeleev Communications
SP - 299-300
IS - 5
VL - 17
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2007_Nagawade,
author = {Rahul R Nagawade and Devanand B Shinde},
title = {Synthesis of amidoalkyl naphthols by an iodine-catalyzed multicomponent reaction of β-naphthol},
journal = {Mendeleev Communications},
year = {2007},
volume = {17},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2007.09.018},
number = {5},
pages = {299--300},
doi = {10.1016/j.mencom.2007.09.018}
}
MLA
Cite this
MLA Copy
Nagawade, Rahul R., and Devanand B Shinde. “Synthesis of amidoalkyl naphthols by an iodine-catalyzed multicomponent reaction of β-naphthol.” Mendeleev Communications, vol. 17, no. 5, Sep. 2007, pp. 299-300. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2007.09.018.

Abstract

Iodine is an efficient catalyst for the multicomponent condensation reaction of β-naphthol, aromatic aldehydes and urea or an amide to afford the corresponding amidoalkyl naphthols in good yields.

References

3.
A facile synthesis of 1,7-dicarbonyl compounds via three-component Michael addition reactions
4.
A simplified green chemistry approach to the Biginelli reaction using ‘Grindstone Chemistry’
Bose A.K., Pednekar S., Ganguly S.N., Chakraborty G., Manhas M.S.
Tetrahedron Letters, 2004
5.
10.1016/j.mencom.2007.09.018_bib2_2
Gohain
Synlett, 2004
7.
Molecular Diversity via a Convertible Isocyanide in the Ugi Four-Component Condensation
Keating T.A., Armstrong R.W.
Journal of the American Chemical Society, 1995
10.
A Facile Synthesis of β-Lactams Based on the Isocyanide Chemistry
Bossio R., Marcos C.F., Marcaccini S., Pepino R.
Tetrahedron Letters, 1997
11.
Studies on isocyanides and related compounds: synthesis of benzo[c]thiophenes by way of acid-induced three-component reactions
Bossio R., Marcaccini S., Pepino R., Torroba T.
Journal of the Chemical Society Perkin Transactions 1, 1996
14.
10.1016/j.mencom.2007.09.018_bib5_3
Chowdari
Synlett, 1906
16.
Modern Variants of the Mannich Reaction
Arend M., Westermann B., Risch N.
Angewandte Chemie - International Edition, 1998
18.
1995 Merck Frosst Award Lecture Quinone methides: relevant intermediates in organic chemistry
Wan P., Barker B., Diao L., Fischer M., Shi Y., Yang C.
Canadian Journal of Chemistry, 1996
20.
Synthesis and Chemistry of Quinone Methide Models for the Anthracycline Antitumor Antibiotics
Angle S.R., Rainier J.D., Woytowicz C.
Journal of Organic Chemistry, 1997
22.
10.1016/j.mencom.2007.09.018_bib7_3
Gardner
J. Am. Chem. Soc., 1959